predictCandidatesTerminal

<code>IRanges</code> of genomic regions with minimal read
coverage required for internal exon prediction

islands

<code>IRanges</code> of splice sites with metadata
columns <dquote>type</dquote> and <dquote>N</dquote>

splicesites

Character string indicating whether terminal exons
should be identified to the left (<dquote>exon_L</dquote>) or right
(<dquote>exon_R</dquote>) of provided splice sites

type

Identify candidate terminal exons based on previously identified
splice sites and regions with sufficient read coverage.

internal

SGSeq is a software package for analyzing splice events from
	     RNA-seq data. Input data are sequence reads mapped to a reference
	     genome in BAM format. Genes are represented as a genome-wide
	     splice graph, which can be obtained from existing annotation or
	     can be predicted from the data. Splice events are identified
	     from the graph and are quantified locally using structurally
	     compatible reads at the start or end of each splice variant.
	     The package includes functions for splice event prediction,
	     quantification, visualization and interpretation.

Leonard Goldstein

SGSeq

Splice event prediction and quantification from RNA-seq data

predictCandidatesTerminal function

<code>IRanges</code> of splice sites with metadata
columns <dQuote>type</dQuote> and <dQuote>N</dQuote>

Character string indicating whether terminal exons
should be identified to the left (<dQuote>exon_L</dQuote>) or right
(<dQuote>exon_R</dQuote>) of provided splice sites

predictCandidatesTerminal: Identify candidate terminal exons

Description

Usage

Arguments

Value